Remote CRA II/Senior – Belgium | Clinical Trials & Sites

KCR Placement; Antwerpen; À distance; EUR 60 000 - 90 000; Plein temps

Résumé du poste

ICON is a global healthcare intelligence and clinical research organisation based in Belgium, offering remote work with travel. This CRA II or Senior CRA role covers oncology, neurology, cardiology, and more, with on-site visits about 8 days per month.

You will monitor sites from start to close-out, manage regulatory submissions (ANSM, CPP), review data, and ensure patient safety. Fluent Dutch/English/French communication is required.

Qualifications

• Master’s degree in life sciences, pharmacy or medicine, or a nursing qualification.
• CRA II: 2+ years of independent monitoring. Senior: 4+ years.
• Strong ICH-GCP and French regulatory knowledge.
• Excellent communication in Dutch, English and French.

Responsabilités

• Monitor sites independently from selection to close-out.
• Handle regulatory submissions and essential documents (ANSM, CPP).
• Review clinical trial data and resolve data queries in a timely manner.
• Protect data quality, ensure protocol compliance, and safeguard patient safety.
• Build strong relationships with investigators and site teams.

Connaissances

Independent monitoring

ICH-GCP knowledge

Multilingual communication

Formation

Master's degree in life sciences/medicine/pharmacy/nursing

Description du poste

ICON is a global healthcare intelligence and clinical research organisation based in Belgium, offering remote work with travel. This CRA II or Senior CRA role covers oncology, neurology, cardiology, and more, with on-site visits about 8 days per month.

You will monitor sites from start to close-out, manage regulatory submissions (ANSM, CPP), review data, and ensure patient safety. Fluent Dutch/English/French communication is required.